Device recall
Z-2190-2015: Mermaid Medical M-Biopsy Coaxial Introducer Needle, Coaxial Needle for M-Biopsy…
FDA device recall · Class II · Mermaid Medical A/S
Key facts
| Recall number (Z-number) | Z-2190-2015 |
|---|---|
| Recall event | 71525 |
| Product | Mermaid Medical M-Biopsy Coaxial Introducer Needle, Coaxial Needle for M-Biopsy 18Gx10cm-PRO-MAG, RX Only. Single packed device in a tyvek pouches. 10 single packed devices in a white carton unit box. The M-Biopsy coaxial needle is used to obtain one or multiple core samples from soft tissue such as… |
| Product code | DWO |
| Recalling firm | Mermaid Medical A/S |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 7, 2015 |
| FEI number | 3007146453 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database